Colon Cancer: Gene >> LHX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263726
Start	180271447:180271447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>T
AA Mutation	p.Lys173Asn(p.K173N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263726
Start	180230558:180230558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29A>G
AA Mutation	p.Glu10Gly(p.E10G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263726
Start	180274376:180274376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544059210
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263726
Start	180274426:180274426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LHX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263726
Start	180271932:180271932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765008063
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263726
Start	180274355:180274355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760897717
CDS Mutation	c.949A>G
AA Mutation	p.Ile317Val(p.I317V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript